Open Access
Subscription Access
Open Access
Subscription Access
Potential Protective Effect of Magnesium Supplementation on Nickel Induced Hepatotoxicity in Albino Wistar Rats
Subscribe/Renew Journal
Nickel is considered one of the most harmful heavy metals on human health. This experimental study was designed to investigate whether magnesium supplementation has any influence on nickel-induced toxicity in albino rats. Twenty one adult rats were divided into three groups of seven animals each group. The first group was used as a control and received saline solution. The second group was administered with nickel sulfate (2.0 mg/100 g, i.p) and the third group was given both nickel sulfate (2.0 mg/100 g, i.p.) and magnesium sulfate (300 mg/kg, i.p) simultaneously on alternate days. Body weight gain was recorded regularly. After 21 consecutive days, cellular functions were evaluated by biochemical and oxidative stress markers. The nickel sulfate-treatment decreased body weight gain in rats. Nickel treatment produced also oxidative injury characterized by an increase in glucose level, enzymes markers activities, lipid profile and total proteins and bilirubin concentrations. Simultaneously, glutathione level (GSH) and catalase activity was diminished in liver tissue. These results are further substantiated with obviously changes in hepato- histoarchithecture. However, the treatment with magnesium ameliorated the previous parameters and resulted in an improvement of the histopathological lesions. Our results suggest that
Keywords
Hepatic Toxicity, Histopathology, Magnesium, Nickel, Oxidative Stress, Rats
User
Subscription
Login to verify subscription
Font Size
Information
- Hassan MU, Chattha MU, Khan I, Chattha MB, Aamer M, Nawaz M, Ali A, Khan MAU, Khan TA. Nickel toxicity in plants: Reasons, toxic effects, tolerance mechanisms and remediation possibilities - a review. Environ Sci Pollut Res. 2019; 26(13):12673–88. PMid: 30924044. https://doi.org/10.1007/s11356-019-04892-x
- Salt DE, Kramer U. Mechanisms of metal hyperaccumulation in plants. Ine. Raskin, I. and Ensley BD, ed. Phytoremediation of toxic metals: Using plants to clean-up the environment. New York: John Wiley and Sons, Inc; 2000. p. 231–46 . 3. Das KK, Reddy RC, Bagoji IB, Das S, Bagali S, Mullur L, Khodnapur, JP, Biradar, MS. Primary concept of nickel toxicity - An overview. J Basic Clin Physiol Pharmacol. 2019; 30(2):141–52. PMid: 30179849. https://doi.org/10.1515/jbcpp-2017-0171
- Das KK, Das GA, Dhundasi SA, Patil AM, Das SN, Ambekar JG. Protective role of L-ascorbic acid on antioxidant defense system in erythrocytes of albino rats exposed to nickel sulfate. BioMetals. 2007; 20(2):177–84. PMid: 16900397. https://doi.org/10.1007/s10534-006-9025-z
- Boulila S, Elfeki A, Oudadesse H, Elfeki H. Substitution effects of a carbonated hydroxyapatite biomaterial against intoxication chloride nickel-exposed rats. Toxicol Mech Methods. 2015; 25(3):155–65. PMid: 25560666. https://doi.org/10.3109/15376516.2014.1003358
- Sun H, Wu W, Guo J, Xiao R, Jiang F, Zheng L, Zhang G. Effects of nickel exposure on testicular function, oxidative stress and male reproductive dysfunction in Spodoptera litura Fabricius. Chemosphere. 2016; 148:178–87. PMid: 26807937. https://doi.org/10.101 6/j.chemosphere.2015.10.068
- Halliwell B. Oxidative stress in cell culture: An under-appreciated problem? FEBS Lett. 2003; 540(1-3):3–6. https://doi.org/10.1016/S0014-5793(03)00235-7
- Gutierrez Iglesias E, Pérez-Arizti JA, Marquez-Ramírez SG, Delgado-Buenrostro NL, Chirino YI, Iglesias GG, Lopez-Marure R. Titanium dioxide nanoparticles induce strong oxidative stress and mitochondrial damage in glial cells. Free Radic Biol Med. 2014; 73:84–94. PMid: 24824983. https://doi.org/10.1016/j.freeradbiomed.2014.04.026
- Costa NMF, Yassuda DH, Sader MS, Fernandes GVO, Soares GDA, Granjeiro JM. Osteogenic effect of tricalcium phosphate substituted by magnesium associated with Genderm membrane in rat calvarial defect model. Mater Sci Eng C. 2016; 61:63–71. PMid: 26838825. https://doi.org/10.1016/j.msec.2015.12.003
- Grober U, Schmidt J, Kisters K. Magnesium in prevention and therapy. Nutrients. 2015; 7(9):8199–226. PMid: 26404370 PMCid: PMC4586582. https://doi.org/10.3390/nu7095388
- Szewczyk B, Poleszak E, Sowa-Kucna M, Siwek M, Dudek D, Ryszewska-Pokrasniewicz B, Radziwon-Zaleska M, Opoka W, Czekaj J, Pilc A, Nowak G. Antidepressant activity of zinc and magnesium in view of the current hypotheses of antidepressant action. Pharmacol Reports. 2008; 60(5):588–99.
- Hartwig A. Role of magnesium in genomic stability. Mutat Res - Fundam Mol Mech Mutagen. 2001; 475(1-2):113–21. https://doi.org/10.1016/S0027-5107(01)00 074-4
- Boujelben M, Ghorbel F, Vincent C, Makni-Ayadi F, Guermazi F, Croute F, El-feki A. Lipid peroxidation and HSP72/73 expression in rat following cadmium chloride administration: Interactions of magnesium supplementation. Exp Toxicol Pathol. 2006; 57(5-6):437–43. PMid: 16616466. https://doi.org/10.1016/j.etp.2006.02.012
- Olatunji LA, Soladoye AO. Increased magnesium intake prevents hyperlipidemia and insulin resistance and reduces lipid peroxidation in fructose-fed rats. Pathophysiology. 2007; 14(1):11–5. PMid: 17187968. https://doi.org/10.1016/j.pathophys.2006.09.004
- Jollow D, Mitchell JR, Zampaglione N, Gillette JR. Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3,4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacology. 1974; 11(3):151–69. PMid: 4831804, https://doi.org/10.1159/000136485
- Aebi H. Catalase in Vitro. Methods Enzymol. 1984; 105(C):121–6. https://doi.org/10.1016/S0076-6879(8 4)05016-3
- Bradford M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976; 72(1-2):248–54. https://doi.org/10.1016/0003-2697(76)90527-3
- Hould R. Techniques d’histopathologie et de cytopathologie. Montreal: Decarie; 1984. p. 400.
- Mujahid M, Hussain T, Siddiqui HH, Hussain A. Evaluation of hepatoprotective potential of Erythrina indica leaves against antitubercular drugs induced hepatotoxicity in experimental rats. J Ayurveda Integr Med. 2017; 8(1):7–12. PMid: 27916487 PMCid: PMC5377476. https://doi.org/10.1016/j.jaim. 2016.10.005
- Dieter MP, Jameson CW, Tucker AN, Luster MI, French JE, Hong HL, Boorma GA. Evaluation of tissue disposition, myelopoietic and immunologic responses in mice after long-term exposure to nickel sulfate in the drinking water. J Toxicol Environ Health. 1988; 24(3):357–72. PMid: 3398077. https://doi.org/10.1080/15287398809531167
- Sidhu P, Garg ML, Dhawan DK. Protective role of zinc in nickel induced hepatotoxicity in rats. Chem Biol Interact. 2004; 150(2):199–209. PMid: 15535990.https://doi.org/10.1016/j.cbi.2004.09.012
- ATSDR (Agency for Toxic Substances and Diseases Registry). Toxicological Profile for Nickel. US Public Heal Serv Agency Toxic Subst Dis Regist [Internet]. 2005 Aug. 397. http://www.atsdr.cdc.gov/ toxprofiles/tp15.pdf
- Rao MV, Parekh SS, Chawla SL. Vitamin-E supplementation ameliorates chromium-and/or nickel induced oxidative stress in vivo. J Heal Sci. 2006; 52(2):142–7. https://doi.org/10.1248/jhs.52.142
- Dormer RL, Kerbey AL, McPherson M, Manley S, Ashcroft SJ, Schofield JG, Randle PH. The effect of nickel on secretory systems. Studies on the release of amylase, insulin and growth hormone. Biochem J. 1974; 140(2):135–42. PMid: 4375956 PMCid: PMC1167985. https://doi.org/10.1042/bj1400135
- Kasprzak KS, Waalkes MP, Poirier LA. Effects of magnesium acetate on the toxicity of nickelous acetate in rats. Toxicology. 1986; 42(1):57–68. https://doi.org/10.1016/0300-483X(86)90092-2
- Cartana J, Arola L. Nickel-induced hyperglycaemia: The role of insulin and glucagon. Toxicology. 1992; 71(1-2):181–92. https://doi.org/10.1016/0300-483X(9 2)90065-M
- Das KK, Das SN. Studies on the role of ascorbic acid on nickel induced hepatic nucleic acid concentrations in rats. J Basic Clin Physiol Pharmacol. 2004; 15(3-4):185–96. PMid: 15803957. https://doi.org/10.1515/JBCPP.2004.15.3-4.185
- Weischer CH, Koerdel W, Hochrainer D. Effects of NiCl2 and NiO in Wistar rats after oral uptake and inhalation exposure respectively. Zentralblatt fur Bakteriol Mikrobiol und Hyg - Abt 1 Orig B Hyg. 1980; 171(4-5):336–51.
- Song Y, He K, Levitan EB, Manson JE, Liu S. Effects of oral magnesium supplementation on glycaemic control in Type 2 diabetes: A meta-analysis of randomized double-blind controlled trials. Diabet Med. 2006; 23(10):1050–6. PMid: 16978367. https://doi.org/10.1111/j.1464-5491.2006.01852.x
- Hussain T, Gupta R, Sweety K, Khan MS, Hussain MS, Arif M, Hussain A, Faiyazuddin M, Rao CV. Evaluation of antihepatotoxic potential of Solanum xanthocarpum fruit extract against antitubercular drugs induced hepatopathy in experimental rodents. Asian Pac J Trop Biomed. 2012; 2(6):45460. https://doi.org/10.1016/S2221-1691(12)60075-6
- Tandon SK, Khandelwal S, Mathur AK, Ashquin M. Preventive effects of nickel on cadmium hepatotoxicity and nephrotoxicity. Ann Clin Lab Sci. 1984; 14(5):390–6.
- Almdal TP, Vilstrup H. Loss of nitrogen from organs in rats induced by exogenous glucagon. Endocrinology. 1988; 123(5):2182–6. PMid: 3049048. https://doi.org/10.1210/endo-123-5-2182
- Hong YC, Paik SR, Lee HJ, Lee KH, Jang SM. Magnesium inhibits nickel-induced genotoxicity and formation of reactive oxygen. Environ Health Perspect. 1997; 105(7):744–8. PMid: 9294721 PMCid: PMC1470112. https://doi.org/10.1289/ehp.97105744
- Stinson TJ, Jaw S, Jeffery EH, Plewa MJ. The relationship between nickel chloride-induced peroxidation and DNA strand breakage in rat liver. Toxicol Appl Pharmacol. 1992; 117(1):98–103. https://doi.org/10.1016/0041-008X(92)90222-E
- Das KK, Dasgupta S. Effect of nickel on testicular nucleic acid concentrations of rats on protein restriction. Biol Trace Elem Res. 2000; 73(2):175–80. https://doi.org/10.1385/BTER:73:2:175
- Chen CY, Wang YF, Lin YH, Yen SF. Nickel-induced oxidative stress and effect of antioxidants in human lymphocytes. Arch Toxicol. 2003; 77(3):123–30. PMid: 12632251. https://doi.org/10.1007/s00204-002-0427-6
- Gstraunthaler G, Pfaller W, Kotanko P. Glutathione depletion and in vitro lipid peroxidation in mercury or maleate induced acute renal failure. Biochem Pharmacol. 1983; 32(19):2969–72. https://doi.org/10.1016/0006-2952(83)90404-5
- Huang C, Li J, Costa M, Zhang Z, Leonard SS, Castranova V, Vallyathan V, Shi, X, Ju, G. Hydrogen peroxide mediates activation of Nuclear Factor ofActivated T cells (NFAT) by nickel subsulfide. Cancer Res. 2001; 61(22):8051–7.
- Djukic-Cosic D, Ninkovic M, Malicevic Z, Matovic V, Soldatovic D. Effect of magnesium pretreatment on reduced glutathione levels in tissues of mice exposed to acute and subacute cadmium intoxication: A time course study. Magnes Res. 2007; 20(3):177–86.
- Li W, Zhao Y, Chou IN. Mg2+ antagonism on Ni2+-induced changes in microtubule assembly and cellular thiol homeostasis. Toxicol Appl Pharmacol. 1996; 136(1):101–11. PMid: 8560462. https://doi.org/10.1006/taap.1996.0012
- Das KK, Saha S. L-ascorbic acid and alpha tocopherol supplementation and antioxidant status in nickel- or lead-exposed rat brain tissue. J Basic Clin Physiol Pharmacol. 2010; 21(4):325–46. https://doi.org/10.1515/JBCPP.2010.21.4.325
- Das KK, Das SN, Das Gupta S. The influence of ascorbic acid on nickel-induced hepatic lipid peroxidation in rats. J Basic Clin Physiol Pharmacol. 2001; 12(3):187–96. PMid: 11762690. https://doi.org/10.1515/JBCPP.2001.12.3.187
- Hans CP, Chaudhary DP, Bansal DD. Effect of magnesium supplementation on oxidative stress in alloxanic diabetic rats. Magnes Res. 2003; 16(1):13–9.
Abstract Views: 183
PDF Views: 0